Friedreich’s Ataxia
Overview of Friedreich’s Ataxia
Friedreich ataxia is a rare condition which is an inherited disease causing progressive nervous system damages and coordination problem. It begins in childhood leading to impaired muscle coordination which worsens over time
Signs and Symptoms of Friedreich’s Ataxia
Vision changes, Loss of hearing, Weak muscles, Lack of reflexes in your legs, Poor coordination or lack of coordination, Speech problems, Involuntary eye movements, Foot deformities such as clubfoot, Difficulty sensing vibrations in your legs and feet
Common Causes of Friedreich’s Ataxia
Genetic factors
Risk Factors of Friedreich’s Ataxia
Family history
Investigation Techniques for Friedreich’s Ataxia
Electromyogram (EMG), Nerve conduction studies, Electrocardiogram (also called EKG or ECG), Echocardiogram, Blood tests to check for elevated glucose levels and vitamin E levels, Magnetic resonance imaging (MRI), Computed tomography (CT) scans
Treatment and Prevention of Friedreich’s Ataxia
5-Hydroxytryptophan, Coenzyme Q, Idebenone, Surgery for scoliosis and foot deformities, Physical therapy, Hearing aids for hearing impairment, Symptomatic & supportive treatment
Available Friedreich’s Ataxia Medicines
No medicines currently available for this condition.
